Revealing Mitochondrial Microenvironmental Evolution Triggered by Photodynamic Therapy
Jing Yue1, Yanting Shen1, Lijia Liang1
1State Key Laboratory of Supramolecular Structure and Materials, Institute of Theoretical Chemistry, College of Chemistry, Jilin University, Changchun 130012, China.
Abstract:
Mitochondrion is one of the most important organelles and becomes a target in many cancer therapeutic strategies. Mitochondrial microenvironments in response to therapeutic methods are the key to understand therapeutic mechanisms. However, they are almost rarely studied. Herein, the mitochondrial microenvironments, including mitochondrial membrane potential (MMP) and reactive oxygen species (ROS) after different photodynamic therapy (PDT) dosages, were monitored by fluorescent imaging and compared among three cell lines (HepG2, MCF-7, and LO2). Furthermore, the fluctuations of intramitochondrial pHs were revealed via a plasmonic mitochondrion-targeting surface-enhanced Raman scattering (SERS) pH nanosensor. Results indicate that the MMP decreases gradually with the ROS generation and the cancerous cells exhibit less response to excess ROS relative to normal cells. On the other hand, the pH value in the mitochondria decreases initially and then increases when the amount of ROS increases. The LO2 cell is preliminarily evidenced to have a higher self-adjustment ability due to its better tolerance to differential intra/extracellular pHs. This study may provide a basis for an in-depth understanding of the mechanisms of the mitochondrial targeting-based PDT therapeutic processes. It is also helpful for more accurate and useful diagnosis according to intramitochondrial microenvironments and improvement on therapy efficiency of cancers.
Insights
Cancer therapy targeting mitochondria is advanced by studying its microenvironment. This research monitored mitochondrial membrane potential, reactive oxygen species, and pH changes during photodynamic therapy, revealing differences between cancer and normal cells.
Area of Science:
- Mitochondrial biology
- Cancer therapy
- Biomedical engineering
Background:
- Mitochondria are crucial organelles and cancer therapeutic targets.
- Understanding mitochondrial microenvironments is key to cancer therapy mechanisms.
- Mitochondrial microenvironments under therapy are understudied.
Purpose of the Study:
- To monitor mitochondrial microenvironments during photodynamic therapy (PDT).
- To compare responses in different cell lines (HepG2, MCF-7, LO2).
- To investigate changes in mitochondrial membrane potential (MMP), reactive oxygen species (ROS), and intramitochondrial pH.
Main Methods:
- Fluorescent imaging to monitor MMP and ROS.
- Surface-enhanced Raman scattering (SERS) nanosensor for intramitochondrial pH.
- Comparative analysis across three cell lines.
Main Results:
- MMP decreases with increasing ROS generation.
- Cancer cells show less response to excess ROS compared to normal cells.
- Intramitochondrial pH initially decreases then increases with ROS.
- LO2 cells exhibit higher self-adjustment ability.
Conclusions:
- This study provides insights into mitochondrial targeting PDT mechanisms.
- Findings aid in understanding cancer cell responses to therapy.
- Results may improve cancer diagnosis and therapy efficiency based on mitochondrial microenvironments.
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